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FDA 510(k)

QUICK SAMPLER HOLDER

K-Number: K120490 · 2012-12-27

ApplicantNipro Medical Corporation
Decision Date2012-12-27
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUICK SAMPLER HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Nipro Medical Corporation. It received FDA 510(k) clearance on 2012-12-27 under 510(k) number K120490. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICK SAMPLER HOLDER?

QUICK SAMPLER HOLDER is a medical device that received FDA 510(k) clearance on 2012-12-27. The listed applicant is Nipro Medical Corporation. The 510(k) number is K120490.

When did QUICK SAMPLER HOLDER receive FDA 510(k) clearance?

QUICK SAMPLER HOLDER received FDA 510(k) clearance on 2012-12-27, under 510(k) number K120490.

Who is the listed applicant for QUICK SAMPLER HOLDER?

The FDA 510(k) record lists Nipro Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUICK SAMPLER HOLDER?

The FDA product code for QUICK SAMPLER HOLDER is JKA.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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